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At least 37 records · Page 2Linked to original sources
PubMed2001

Initial tissue response to anti-washout apatite cement in the rat palatal region: comparison with conventional apatite cement.

Initial tissue response to anti-washout apatite cement (aw-AC) in the palatal region was studied. Conventional apatite cement (c-AC) was employed as a control material. Bone defects generated in the rat palatal region, where complete hemostasis is difficult to effect, were filled with both cement types and examined histologically for up to 8 weeks. At 1-week postfilling, a portion of the c-AC had washed out, resulting in slight inflammation and severe foreign-body response. The degree of foreign-body response to c-AC was reduced over time; however, foreign-body response continued to be in evidence 8 weeks after surgery. As a result, poor bone formation was observed in the case of c-AC at 8 weeks post-surgery. In contrast, aw-AC set well, maintained its shape at implantation, and caused little foreign-body response. Osteoblasts were observed at 2 weeks following surgery. Moreover, the bone defect was completely covered with new bone at 8 weeks post-surgery. This observation suggests that aw-AC may be used without complication in cases where complete hemostasis is difficult to achieve, that is, where the use of c-AC is contraindicated.

Animals↗
PubMed1985

Long-lived radicals in irradiated apatites of biological interest: an e.s.r. study of apatite samples treated with 13CO2.

Hydroxyapatite is used as a model for studying radical formation in the mineral compartment of irradiated calcified tissues. Treating this material with 13C-enriched CO2 confirms that radiogenic long-lived radicals correspond to carbon centred species. It is shown, however, that these radicals are not located on the carbonate ions which substitute either the phosphate or the hydroxyl groups. The conditions which allow the formation and the trapping of these radicals are investigated (role of humidity, CO2 and temperature) and this paramagnetic species is identified as CO-2 adsorbed at the surface of apatite crystallites.

Carbon Dioxide↗
PubMed1990

[Fluoride ions and apatite recrystallization of apatite in enamel].

The authors discuss the basic process on which the principle of fluoridation in based--i.e. the mutual exchange of F- ions and the OH- group in hydroxyapatite of enamel. Model investigations assessing the energy difference between hydroxyapatite and F- and fluorapatite and the OH- group indicate that fluorapatite tends to release steadily fluoride ions and to change into hydroxyapatite. This tendency, apparently inopportune from the aspects of caries prevention, ensures, however, a permanent low F- level above the enamel surface. The presence of F- ions facilitates recrystalization of apatite in the initial caries stage. The investigation tries to throw new light, from the point of view of theoretical chemistry at a molecular level, on the mechanism of remineralization, one of the most important ways which implements the preventive action of fluoride.

Crystallization↗
PubMed1989

[Self-setting apatite cement. VII. Barium-apatite as radio-opaque medium].

Addition of barium hydroxyapatite (BaAp) successfully bestowed clinically acceptable radioopacity to the self-setting apatite cement consisting of an equimolar mixture of tetracalcium phosphate and dicalcium phosphate dihydrate. To accelerate the setting reaction which was retarded by Ba2+ released from BaAp at a lower pH during first stage of spatulation with 20 mM phosphoric acid, calcium hydroxyapatite (CaAp) was added to the cement mixture. At about 20 wt% of BaAp and 20 wt% CaAp, the setting reaction proceeded at a neutral or weak alkaline pH, which is one of the most promising aspects of the self-setting cement and assures that this type of cement may be the least irritating of the dental cements presently available. The cement spatulated at L/P = 0.4 set within 10 minutes and its radiopacity was comparable to or more than that of tooth enamel. The wet compressive strength of the set cement stored for one day in synthetic saliva at 37 degrees C was approximately 100 kgf/cm2. Although this value is almost one fourth that of 40 wt% CaAp cement, this cement appears to be strong enough to apply as root canal filling material.

Barium↗
PubMed1990

Ultrastructure, morphology and crystal growth of biogenic and synthetic apatites.

The morphology, structure and crystal growth of apatite crystals isolated from calcified turkey tendon and synthetic carbonated apatites have been examined using high resolution transmission electron microscopy. The biogenic apatite consisted of small (35 x 20 x 5 nm) platelike crystals. Despite their irregular shape and ill-defined edges, individual particles were single domain crystals. Lattice images recorded from isolated turkey tendon crystals indicated that the crystallographic c-axis (0001) of apatite lies in the plane of the plate and parallel to the length of the crystallites. Lattice images suggested that the top face corresponds to the (1100) face of carbonated apatite. Lattice fringes observed in platelike crystallites viewed from the side corresponded to the projection of the apatite structure viewed along the [1120] direction. Thus, it can be argued that crystal growth is constrained along the [1100] direction, extends laterally along the [1120] direction, and is maximal along the [0001] direction. This latter direction is aligned with the collagen fiber axis. A mean length to width ratio (1.7) was determined by systemically measuring the maximum distances parallel and perpendicular to the c-axis identified from lattice images of the crystals. Similar information was obtained from lattice images of crystals located in collagen fibres. This confirmed that the morphological and structural features of isolated turkey tendon apatite crystals correlate directly with the in vivo crystallochemical characteristics of apatite. Crystals of synthetic carbonated apatite prepared at 37 degrees C were also platelike and, although generally much larger, had length to width ratios comparable with the turkey tendon apatite. The synthetic carbonated apatites were noticeably more sensitive to radiolytic damage than the turkey tendon crystals. The crystallographic c-axis of the inorganic particles was aligned parallel with the long, physical axis of the plate and the top face was identified as (1100). Similar data were also obtained from noncarbonated synthetic apatite samples. The results of the present study offer critical information about the crystal growth of individual carbonated apatite crystals in calcified turkey tendon and its relationship to the morphology of the crystallites. As similar growth characteristics are expressed in synthetic analogues, the data bring into question the putative regulatory role of the collagen-based matrix upon the nucleation and growth of biogenic apatite.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1990

[Dissolution and radio-opacity of apatite cement].

Dissolution and remineralization behaviors of self-setting apatite cement is organic acids and synthetic saliva and the effect of barium apatite (BaAp)on physicochemical and mechanical properties of the apatite cement were investigated. One-week solubility of several types of apatite cement was considerably smaller than that of commercially available dental cements in 1 mM of acetic, lactic and citric acids (pH4.0 at 37 degrees C). For example, the one-week solubility in citric acids was less than 4.5%. To investigate the dissolution behavior of the apatite cement in detail, two types of 45Ca labeled apatite cement were prepared. In one, the seed apatite was labeled with 45Ca(45Ca-HAp cement) and in the other the matrix apatite was labeled with 45Ca through use of 45Ca-DCPD (45Ca-DCPD cement). Solubility, estimated from the concentration of 45Ca released in 1mM of the organic acid was approximately zero for 45Ca-HAp cement, whereas the solubility of 45Ca-DCPD cement was similar to that of unlabeled cements. This suggests cat dissolution of the matrix apatite governs dissolution of the set cement. In synthetic saliva, the solution phosphate decreased with time once the set cement was introduced to the solution, whereas the solution calcium increased. The former finding suggests that some phosphate compounds precipitated in the synthetic saliva and the latter finding indicates that some portion of the set cement dissolved. The thermodynamic analysis of the solution compositions strongly suggests that remineralization is a major process and dissolution a minor one. In fact, in systhetic saliva labeled with 45Ca having a degree of supersaturation with respect to apatite comparable to rest saliva, 45Ca concentration in solution decreased once the cement pellet was introduced. This finding clearly suggests that the set apatite cement has the ability to remineralize but not to dissolve in synthetic saliva even if the degree of supersaturation with respect to apatite is relatively low. Addition of barium hydroxyapatite (BaAp) successfully bestowed clinically acceptable radio-opacity to the apatite cement. To accelerate the setting reaction which was retarded by Ba2+ released from BaAp at a lower pH during the first stage of spatulation, calcium hydroxyapatite (CaAp) was added to the cement mixture. At 20wt% of BaAp and 20wt% CaAp, the setting reaction proceeded at a neutral or weak alkaline pH, which is one of the most promising aspects of the apatite cement. The cement spaturated at L/P = 0.4 set within 10 minutes and its radio-opacity was comparable to or more than that of tooth enamel.(ABSTRACT TRUNCATED AT 400 WORDS)

Acetates↗
PubMed2004

Roughness and bonding strength of bioactive apatite layer on dental implants.

This study examined the roughness and bonding strength of the chemical-made apatite layer in comparison with the titanium surface and the plasma-sprayed apatite. Commercially pure titanium plates were heated and chemically treated to deposit crystalline apatite on their surface. The roughness of the titanium surface of the original samples and the apatite surface was analyzed by a roughness surface tester. A scratch test was used to compare the adhesion of the chemical apatite layer to the titanium with the adhesion of a plasma-sprayed layer. A dense bone-like apatite layer was formed on the surface of the titanium by a simple chemical method. The surface roughness test showed that the chemical apatite coating increased the roughness of the samples. The scratch test showed that the bonding strength of the chemical-made apatite coatings to the titanium substrate was higher than the plasma-sprayed apatite coatings. The apatite layer produced by chemical treatment did not show a lower roughness than the titanium substrate. This chemical apatite layer also bonded tighter to the titanium than the plasma-sprayed apatite. This chemically made apatite coating is expected to provide a long-term implant-bone fixation.

Coated Materials, Biocompatible↗
PubMed1999

A comparative infrared spectroscopic study of hydroxide and carbonate absorption bands in spectra of shark enameloid, shark dentin, and a geological apatite.

The purpose of the present work was to investigate the infrared (IR) spectrum of shark enameloid, especially with regard to hydroxide and carbonate bands. With thin sections placed directly in the IR beam it was possible to get high concentrations of ions without interfering effects from a dispersion medium (e.g., alkali halides). For comparison, spectra of shark dentin and a geo-apatite were also recorded. In spectra of shark enameloid and geo-apatite medium strong hydroxide absorption bands were found around 3535 cm(-1), and in shark dentin and geo-apatite spectra weak shoulders were observed at about 3570 cm(-1). Hydroxide libration bands at about 740 cm(-1) were found in shark enameloid and geo-apatite spectra; in the latter, also a band at 680 cm(-1). Carbonate bands were found in shark enameloid spectra at 1480 (weak shoulder), 1453, 1423, and 868 cm(-1). In shark dentin spectra there were carbonate bands at 1452, 1417, and 875 cm(-1), and probably also a carbonate band at about 1530 cm(-1) overlapped by an amide II band. Weak carbonate bands were also found in the spectra of the geo-apatite at 1452 cm(-1), and at about 1425 and 880 cm(-1). The relative intensities of the bands at 1453 cm(-1) (contributed from A and B sites) and around 1420 cm(-1) (B sites) changed from shark enameloid to shark dentin, and also from shark enameloid to the geo-apatite. More A sites seem to be occupied by carbonate in shark dentin than in shark enameloid, supposedly owing to fluoride occupation of A sites in shark enameloid. In geo-apatite and shark enameloid there are hydroxide ions hydrogen bonded to fluoride. Both shark enameloid and the geo-apatite are fluoride rich, and geo-apatite seems to have the highest fluoride concentration. There are, however, indications that the hydroxide concentration is also higher in the geo-apatite than in shark enameloid. This can be explained by the much higher carbonate content, and partly also by the higher water content in shark enameloid. There are A sites in geo-apatite and probably also in shark enameloid which are occupied by carbonate, but the proportion of occupied A sites relative to occupied B sites is greater in geo-apatite than in shark enameloid. This difference can be explained by the preference of A sites when the carbonate concentration is very low. On the other hand, for greater amounts of carbonate such as we have in shark enameloid, B sites are preferred.

Animals↗
PubMed1989

Stability and mutual conversion of enamel apatite and brushite at 20 degrees C as a function of pH of the aqueous phase.

By calculation, apatite is more soluble than brushite at low pH and less soluble at high pH. Apatite, therefore should be able to transform spontaneously to brushite at low pH and brushite to apatite at high pH. The aim was to describe this mutual conversion as related to the aqueous phase composition. Powdered enamel, brushite or 1:1 mixtures of the two salts were suspended in distilled water for up to 12 weeks at 20 degrees C, pH was adjusted to 4, 5, 6, 7, 8, 9 or 10 by drops of perchloric acid or potassium hydroxide. The calcium and the phosphate concentrations and pH were determined, and the nature of the calcium phosphate powder was examined by X-ray diffraction. At pH 8 and above, brushite was invariably converted to apatite, whilst it was transformed to octacalcium phosphate at pH 7. In the pH range 6-4 brushite was not converted to apatite and enamel apatite was not transformed to brushite spontaneously within 2 months. In the enamel apatite suspensions, the apatite ion product altered with pH, which explained why apatite did not transform to brushite at pH 5-4. At pH 3.7, however, the enamel apatite was converted to brushite. No transformation of apatite to brushite was identified in apatite-brushite mixtures at pH 6-4. Supplementary experiments showed that ethanol, used as an agent for removal of water, salted out the water-free dicalcium phosphate, monetite.

Apatites↗
PubMed2005

The effect of calcium fluoride (CaF(2)) on the chemical solubility of an apatite-mullite glass-ceramic material.

OBJECTIVE: To assess the effect of varying CaF(2) on the chemical solubility of apatite-mullite glass-ceramic (G-C) materials in both the glassy and crystallized states. METHODS: Apatite-mullite forming glasses used in this study are ionomer cement derivatives based on the general formula (4.5SiO(2)-3Al(2)O(3)-1.5P(2)O(5)-3CaO-XCaF(2)). Six glass formulations were produced where X=0.5, 1, 1.5, 2, 2.5 and 3, and called HG1-6, respectively. Batches were melted in covered silliminite crucibles in a furnace overnight at 1050 degrees C, then at 1450 degrees C for 2h, before quenching in water. The six glass compositions were analyzed using differential thermal analysis (DTA), X-ray diffraction (XRD) and X-ray fluorescence spectrometry (XRF). Thirty discs (2mm thick and 12 mm diameter) were produced per glass using the lost wax casting technique. Ten were left as cast and 10 heat treated to either apatite or apatite-mullite. Solubility testing was carried out according to International Standard BS EN ISO 6872 1999 and the mass difference in solubility calculated as mug/cm(2). A lithium disilicate G-C system was used as a control material. RESULTS: All compositions formed glasses and on heat treatment could form apatite and apatite-mullite. The as-cast glass samples were the most soluble followed by the apatite samples. The apatite-mullite G-C was significantly less soluble than the other two phases (p<0.05) for all six compositions. The control material was significantly less soluble than all the HG glass-ceramic compositions for every phase (p<0.05). Decreasing the CaF(2) content (3-0.5 mol%) led to a decrease in solubility, without affecting the ability of the material to form apatite and apatite-mullite phases. SIGNIFICANCE: Increasing the CaF(2) content increases the chemical solubility for the glass, apatite G-C and apatite-mullite G-C phases. The solubility values obtained show that all the compositions, as cast and heat treated would be suitable for use as core ceramics.

Aluminum Silicates↗
PubMed1993

Crystallographic morphology of heterogeneous fluoridated carbonate apatites.

Carbonate-containing fluoridated apatites were synthesized with two different modes of fluoride incorporation: by supplying F-free solution initially, followed by a F-containing solution; and with the order of supply of these solutions reversed. Both of these heterogeneously synthesized fluoridated CO3 apatites showed typical apatitic x-ray diffraction patterns; and both had similar total fluoride contents (0.87 +/- 0.07 and 0.94 +/- 0.03 mmol/g, respectively), i.e., half of the maximum fluoride content of fluorapatite. However, they differed considerably in their crystallographic properties. The 300 reflection peaks of both apatites were split, and their patterns were slightly different. In the former, SEM observation revealed capsule-like crystals with a rounded hexagonal shape. However, the latter had many small crystals, similar to those of homogeneous CO3 apatite, adhering to the larger hexagonal crystals, which were also similar to homogeneous fluorCO3 apatite. Wavelength-dispersive spectroscopy attached to the SEM showed a higher fluoride intensity in the former spectrum than the latter. These results suggest that two different types of heterogeneous fluoridated CO3 apatites were formed, CO3 apatite covered with fluorCO3 apatite, and fluorCO3 apatite covered with CO3 apatite. The simple two-step supply system used in this study is helpful for the study of complicated heterogeneous formation of apatites.

Apatites↗